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FDA 510(k)

MEDO BUBBLE BATH MA-80, 400, 600 & 700

K-Number: K844064 · 1985-01-23

ApplicantMedo U.S.A., Inc.
Decision Date1985-01-23
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDO BUBBLE BATH MA-80, 400, 600 & 700 is the device name listed in this FDA 510(k) record. The listed applicant is Medo U.S.A., Inc.. It received FDA 510(k) clearance on 1985-01-23 under 510(k) number K844064. The device is classified under product code ILJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDO BUBBLE BATH MA-80, 400, 600 & 700?

MEDO BUBBLE BATH MA-80, 400, 600 & 700 is a medical device that received FDA 510(k) clearance on 1985-01-23. The listed applicant is Medo U.S.A., Inc.. The 510(k) number is K844064.

When did MEDO BUBBLE BATH MA-80, 400, 600 & 700 receive FDA 510(k) clearance?

MEDO BUBBLE BATH MA-80, 400, 600 & 700 received FDA 510(k) clearance on 1985-01-23, under 510(k) number K844064.

Who is the listed applicant for MEDO BUBBLE BATH MA-80, 400, 600 & 700?

The FDA 510(k) record lists Medo U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDO BUBBLE BATH MA-80, 400, 600 & 700?

The FDA product code for MEDO BUBBLE BATH MA-80, 400, 600 & 700 is ILJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Medo U.S.A., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K841235MEDO MEDOMER MBF-100 II

Related Devices (Code: ILJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K110994PARKER 500Arjohuntleigh, Inc.K082951IMMERSION HYDROBATHArjo Hospital Equipment ABK052479MBATH 1000 (60)Enneking Medical, Inc.K040772PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEMPenner Manufacturing, Inc.K012061SUPERIOR BATH, MODEL 6300Penner Manufacturing, Inc.K012057CASCADE BATH, MODEL 6900Penner Manufacturing, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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